Literature DB >> 1083196

[Partial deletion of the short arm of chromosome 8].

L Taillemite, J Channarond, H Tinel, N Muliez, C H Roux.   

Abstract

Mesh：

Year:  1975        PMID： 1083196

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


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  9 in total

1.  New chromosomal malformation syndromes. I. Partial monosomy 8p. An attempt to establish a new chromosome deletion syndrome.

Authors:  A Rodewald; S Stengel-Rutkowski; P Schulz; H Cleve
Journal:  Eur J Pediatr       Date:  1977-04-26       Impact factor: 3.183

2.  Deletion of the long arm of chromosome 8 resulting from a de novo translocation t(4;8) (q13;q213).

Authors:  B Dallapiccola; L Santoro; S Trabace; M Ramenghi; P Mastroiacovo; E Gandini
Journal:  Hum Genet       Date:  1977-09-22       Impact factor: 4.132

3.  Small structural changes of chromosome 8. Two cases with evidence for deletion.

Authors:  C Beighle; L E Karp; J W Hanson; J G Hall; H Hoehn
Journal:  Hum Genet       Date:  1977-08-31       Impact factor: 4.132

4.  Partial monosomy 8p with minimal dysmorphic signs.

Authors:  E Blennow; K Bröndum-Nielsen
Journal:  J Med Genet       Date:  1990-05       Impact factor: 6.318

5.  Interstitial deletion of the long arm of chromosome 8. Karyotype: 46,XY,del(8)(q21).

Authors:  J P Fryns; N Logghe; M Van Eygen; H Van Der Berghe
Journal:  Hum Genet       Date:  1979-04-17       Impact factor: 4.132

6.  Ring chromosome 8 in a boy with multiple congenital abnormalities and mental retardation.

Authors:  A J Hamers; C van Kempen
Journal:  J Med Genet       Date:  1977-12       Impact factor: 6.318

7.  10p- syndrome associated with multiple chromosomal abnormalities.

Authors:  F Prieto; L Badia; J A Moreno; P Barbero; F Asensi
Journal:  Hum Genet       Date:  1978-12-18       Impact factor: 4.132

8.  The 8p- syndrome.

Authors:  J A Reiss; P M Brenes; J Chamberlin; R E Magenis; E W Lovrien
Journal:  Hum Genet       Date:  1979-03-12       Impact factor: 4.132

9.  Monosomy 8p: an easily overlooked syndrome.

Authors:  A H Bröcker-Vriends; P D Mooij; F van Bel; G C Beverstock; J J van de Kamp
Journal:  J Med Genet       Date:  1986-04       Impact factor: 6.318
  9 in total

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